Congenital cataract
Symptom Information:
Symptom ID: | HPO:0000519 | ||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the eye(HPO:0000478) Abnormal eye morphology(HPO:0012372) Abnormality of the globe(HPO:0012374) Abnormality of the anterior segment of the globe(HPO:0004328) Abnormality of the lens(HPO:0000517) Cataract(HPO:0000518) Congenital cataract(HPO:0000519) MedDRA: Infections and infestations(MedDRA:10021881) Viral infectious disorders(MedDRA:10047438) Rubella viral infections(MedDRA:10039270) Congenital cataract(HPO:0000519) |
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Database Frequency: | 73 / 7739 | ||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
3-phosphoglycerate dehydrogenase deficiency | (Orphanet:79351) |
ADAMS-OLIVER SYNDROME 2 | (OMIM:614219) |
ATAXIA-MICROCEPHALY-CATARACT SYNDROME | (OMIM:208870) |
Absence deformity of leg - cataract | (Orphanet:2310) |
Autosomal dominant Kenny-Caffey syndrome | (Orphanet:93325) |
Autosomal recessive palmoplantar keratoderma and congenital alopecia | (Orphanet:1366) |
Autosomal recessive spastic paraplegia type 45 | (Orphanet:320396) |
Autosomal recessive spastic paraplegia type 46 | (Orphanet:320391) |
CARDIOFACIOCUTANEOUS SYNDROME 4 | (OMIM:615280) |
CATARACT 1, MULTIPLE TYPES | (OMIM:116200) |
CATARACT 10, MULTIPLE TYPES | (OMIM:600881) |
CATARACT 16, MULTIPLE TYPES | (OMIM:613763) |
CATARACT 17, MULTIPLE TYPES | (OMIM:611544) |
CATARACT 3, MULTIPLE TYPES | (OMIM:601547) |
CATARACT 37 | (OMIM:614422) |
CATARACT 38 | (OMIM:614691) |
CATARACT 39, MULTIPLE TYPES | (OMIM:615188) |
CATARACT 4, MULTIPLE TYPES | (OMIM:115700) |
CATARACT 41 | (OMIM:116400) |
CATARACT 42 | (OMIM:115900) |
CATARACT 6, MULTIPLE TYPES | (OMIM:116600) |
CATARACT, CONGENITAL, WITH MENTAL IMPAIRMENT AND DENTATE GYRUS ATROPHY | (OMIM:607674) |
CATARACT, TOTAL CONGENITAL | (OMIM:116700) |
CATARACTS, CONGENITAL, WITH SENSORINEURAL DEAFNESS, DOWN SYNDROME-LIKEFACIAL APPEARANCE, SHORT STATURE, AND MENTAL RETARDATION | (OMIM:601088) |
CODAS syndrome | (Orphanet:1458) |
Cataract - ataxia - deafness | (Orphanet:1368) |
Cataract - nephropathy - encephalopathy | (Orphanet:1380) |
Cataract with Y-shaped suture opacities | (Orphanet:98985) |
Cataract, Coppock-like | (Orphanet:98986) |
Cataract, Hutterite type | (Orphanet:98987) |
Cataract-microcornea syndrome | (Orphanet:1377) |
Congenital cataract, Volkmann type | (Orphanet:98983) |
Congenital cataract-hearing loss-severe developmental delay syndrome | (Orphanet:300313) |
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome | (Orphanet:1369) |
Congenital cataracts - facial dysmorphism - neuropathy | (Orphanet:48431) |
Congenital osteogenesis imperfecta - microcephaly - cataracts | (Orphanet:2772) |
Early-onset non-syndromic cataract | (Orphanet:217052) |
FECHTNER SYNDROME | (OMIM:153640) |
Familial vascular leukoencephalopathy | (Orphanet:36383) |
GROWTH FAILURE, MICROCEPHALY, MENTAL RETARDATION, CATARACTS, LARGEJOINT CONTRACTURES, OSTEOPOROSIS, CORTICAL DYSPLASIA, AND CEREBELLARATROPHY | (OMIM:608278) |
HEC syndrome | (Orphanet:2119) |
Hypomyelination - congenital cataract | (Orphanet:85163) |
Kenny-Caffey syndrome | (Orphanet:2333) |
Knobloch syndrome | (Orphanet:1571) |
MELAS | (Orphanet:550) |
MOVED TO 302200 | (OMIM:302300) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 1 | (OMIM:613155) |
Marinesco-Sjögren syndrome | (Orphanet:559) |
Marshall syndrome | (Orphanet:560) |
Micro syndrome | (Orphanet:2510) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Nance-Horan syndrome | (Orphanet:627) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Oculofaciocardiodental syndrome | (Orphanet:2712) |
PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, AND NEURODEGENERATIONSYNDROME | (OMIM:606721) |
PEROXISOME BIOGENESIS DISORDER 14B | (OMIM:614920) |
PHACE syndrome | (Orphanet:42775) |
PHEOCHROMOCYTOMAPHEOCHROMOCYTOMA, SUSCEPTIBILITY TO | (OMIM:171300) |
PUPILLARY MEMBRANE, PERSISTENCE OF | (OMIM:178900) |
Partial congenital cataract | (Orphanet:98992) |
Porencephaly-microcephaly-bilateral congenital cataract syndrome | (Orphanet:306547) |
RETINITIS PIGMENTOSA 62 | (OMIM:614181) |
Rhizomelic chondrodysplasia punctata | (Orphanet:177) |
Rhizomelic chondrodysplasia punctata type 1 | (Orphanet:309789) |
Scalp-ear-nipple syndrome | (Orphanet:2036) |
Spastic ataxia - corneal dystrophy | (Orphanet:2572) |
Spastic paraplegia 64, autosomal recessive | (OMIM:615683) |
Vici syndrome | (Orphanet:1493) |
WARBURG MICRO SYNDROME 1 | (OMIM:600118) |
WARBURG MICRO SYNDROME 2 | (OMIM:614225) |
WARBURG MICRO SYNDROME 4 | (OMIM:615663) |
X-linked Alport syndrome | (Orphanet:88917) |
[DEL] SENGERS SYNDROME | (OMIM:212350) |